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Updated: Jan 23, 2026

Gene Regulation and Targeted Therapy in Gastric Cancer Peritoneal Metastasis: Radiological Findings from Dual Energy CT and PET/CT
Published on: January 22, 2018
MiR-876-5p regulates gastric cancer cell proliferation, apoptosis and migration through targeting WNT5A and MITF
Zhenglei Xu1, Zhichao Yu1, Qinghong Tan1
1Department of Gastroenterology, The Second Clinical Medical College (Shenzhen People's Hospital), Jinan University, Shenzhen 518000, Guangdong, China.
Abstract:
MicroRNAs (miRNAs) are reported to play critical roles in various cancers. Recently, mounting miRNAs are found to exert oncogenic or tumor inhibitory role in gastric cancer (GC), however, their potential molecular mechanism in GC remains ill-defined. Currently, we aimed to elucidate the functional and mechanistic impacts of a novel miRNA on GC cellular process. The significant down-regulation of miR-876-5p in GC cells attracted our attention. In function, we performed gain-of-function assays and found that miR-876-5p overexpression repressed proliferative, anti-apoptotic and migratory abilities and epithelial-mesenchymal transition (EMT) of GC cells. By applying bioinformatics prediction and mechanism experiments, we verified that miR-876-5p could double-bind to the 3' untranslated regions (3'UTRs) of Wnt family member 5A (WNT5A) and melanogenesis associated transcription factor (MITF), thus regulating their mRNA and protein levels. Both WNT5A and MITF were highly expressed in GC cells. Additionally, we conducted loss-of-function assays and confirmed the oncogenic roles of WNT5A and MITF in GC. Finally, rescue assay uncovered a fact that miR-876-5p suppressed GC cell viability and migration, but induced cell apoptosis via targeting WNT5A and MITF. Taken together, we might offer a valuable evidence for miR-876-5p role in GC development.
Insights
MicroRNA-876-5p (miR-876-5p) suppresses gastric cancer (GC) progression by inhibiting proliferation, migration, and epithelial-mesenchymal transition. It targets WNT5A and MITF, revealing a novel mechanism in GC development.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) play crucial roles in various cancers, including gastric cancer (GC).
- The specific molecular mechanisms of many miRNAs in GC remain unclear.
- miR-876-5p was found to be significantly downregulated in GC cells.
Purpose of the Study:
- To investigate the functional and mechanistic roles of miR-876-5p in gastric cancer.
- To elucidate the molecular targets and pathways regulated by miR-876-5p in GC.
Main Methods:
- Gain-of-function assays to assess miR-876-5p overexpression effects.
- Bioinformatics prediction and mechanism experiments to identify direct targets.
- Loss-of-function assays for WNT5A and MITF.
- Rescue assays to confirm the regulatory pathway.
Main Results:
- Overexpression of miR-876-5p repressed GC cell proliferation, anti-apoptosis, migration, and epithelial-mesenchymal transition (EMT).
- miR-876-5p was verified to target both WNT5A and MITF mRNA and protein.
- WNT5A and MITF were highly expressed in GC cells and exhibited oncogenic roles.
- miR-876-5p suppressed GC cell viability and migration while inducing apoptosis by targeting WNT5A and MITF.
Conclusions:
- miR-876-5p acts as a tumor suppressor in gastric cancer.
- The miR-876-5p/WNT5A/MITF axis represents a novel regulatory pathway in GC.
- This study provides evidence for the potential therapeutic role of miR-876-5p in GC treatment.
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